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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659350Generated: November 2, 2026

1-Nitro-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazoline → 1-Amino-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazoline

https://huagongshe.com/reaction/1659350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Nitro-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazolineHCID 13175675—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Amino-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazolineHCID 1317568584.6%

Reaction Steps

27.1 g (0.1 mole) of 1-nitro-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazoline are hydrogenized in ethanol in the presence of palladium/carbon catalyst. When the reduction is complete, the catalyst is removed by filtration and the filtrate is evaporated in an inert atmosphere under reduced pressure. 20.5 g (81%) of 1-amino-5-methyl-6-acetyl-5,6-dihydropyrazolo[1,5-c]quinazoline are obtained as white crystals. M.p.: 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04303660
Source datasetuspto-grants-1981_12
ORD IDord-8fb6098d93244619b7c8d45ab751056c
Source noteuspto-grants-1981_12